• Study Resource
  • Explore Categories
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
formula - eduBuzz.org
formula - eduBuzz.org

... • How does the size of a molecule change as the boiling point of a fraction increases? • What are some of the fractions distilled from crude oil and what are they are used for? • What are the typical numbers of carbon atoms in each of the fractions? ...
Ethers, Sulfides, Epoxides
Ethers, Sulfides, Epoxides

... The last step which produces the haloform, HCX3 only occurs if there is an a methyl group, a methyl directly attached to the carbonyl. If done with iodine then the formation of iodoform, HCI3, a bright yellow precipitate, is a test for an a methyl group (iodoform test). ...
Alcohols
Alcohols

... Monohydroxy alcohols are classified according to type of carbon bearing OH into three types: • 1ry alcohols: in which OH attach with 1ry carbon e.g. RCH2OH • 2nd alcohols: in which OH attach with 2nd carbon e.g. R2CHOH • t-alcohols : in which OH attach with tertiary carbon e.g. R3COH ...
12. 16 Physical Properties of Alkanes and Cycloalkanes.
12. 16 Physical Properties of Alkanes and Cycloalkanes.

...  Be able to determine molecular formula from, condensed, structural, a line-angle formula Know IUPAC nomenclature for simple (unbranched) alkanes  Be able to draw constitutional isomers (Lewis structures or condensed formulas as specified) given the molecular formula  Know the names of common alk ...
Lectures 15, 16 and 17
Lectures 15, 16 and 17

... • Grignards react with CO2 to give carboxylic acids after protonation with aqueous acid. • This reaction is called carboxylation. • The carboxylic acid formed has one more carbon atom than the Grignard reagent from which it was prepared. ...
REVISED Review 3 - Bonham Chemistry
REVISED Review 3 - Bonham Chemistry

... * 32. Progesterone, which is present in humans as a single stereoisomer, has six stereocenters. Human progesterone is one of how many possible stereoisomers for this structure? ...
Chapter 25. The Chemistry of Life: Organic and Biological Chemistry
Chapter 25. The Chemistry of Life: Organic and Biological Chemistry

... • Amines are important organic bases. • They contain the functional groups –NH2, –NHR or –NR2. • “R” groups are groups consisting of carbon-carbon and carbon-hydrogen bonds. Some molecules contain both an acidic and a basic group. ...
Chapter 1-
Chapter 1-

... Solved Problem: Synthesize the following compound using an alcohol of not more than 4 carbons as the only organic starting material ...
Chapter 18 Reactions of aromatics
Chapter 18 Reactions of aromatics

... carbocations are too hard to form) • Will not work with rings containing an amino group substituent or a strongly electron-withdrawing group ...
Chapter 12 Alcohols from Carbonyl Compounds: Oxidation
Chapter 12 Alcohols from Carbonyl Compounds: Oxidation

... Solved Problem: Synthesize the following compound using an alcohol of not more than 4 carbons as the only organic starting material ...
Lecture 18
Lecture 18

... to be reasonable soluble in water so that it can be transported through the blood. Since amines are weak bases, they are often converted to salts with some acid and therefore may oral drugs have amine salts as part of their structure. One reason for their presence is that they confer some water solu ...
Organic Chemistry
Organic Chemistry

... dilute NaOH sol’n), CN-, NH3 and H2O. The nucleophiles are attracted to the δ+ carbon atom and substitute the halogen atom in halogenoalkanes. Primary halogenoalkanes react by an SN2 mechanism. Tertiary halogenoalkanes react by an SN1 mechanism. HL ...
Organic Reactions
Organic Reactions

... Ability to distinguish reactants and products in a reaction Naming and identifying organic compounds Ability to distinguishing between saturated and unsaturated hydrocarbons Naming and recognizing functional groups in organic compounds ...
Elimination Reactions
Elimination Reactions

... 3. Weakly basic, weak nucleophiles, like H2O, EtOH, CH3COOH, etc., cannot react unless a C+ forms. This only occurs with 2° or 3° substrates. Once the C+ forms, both SN1 and E1 occur in competition. The substitution product is usually predominant. 4. High temperatures increase the yield of eliminati ...
chem 464l survival guide
chem 464l survival guide

... hydrogen bond – a weak electrostatic attraction between one electronegative atom (oxygen, nitrogen, etc.) and a hydrogen atom covalently linked to a second electronegative atom ...
Unit 2 Review: Answers: Review for Organic Chemistry Unit Test 2
Unit 2 Review: Answers: Review for Organic Chemistry Unit Test 2

... 3. Be able to use physical or chemical properties to distinguish between organic substances. For example, identify one physical or chemical property you could use to distinguish between the following pairs of organic substances: a) 2-butanol and 2-methyl-2-propanol: • 2-butanol is a secondary alcoho ...
Answers
Answers

... of hydroxide is needed. Draw a full mechanism to explain. (Hint: Before the elimination takes place, another reaction type we have learned takes place more quickly.) ...
Revision Y12 Chemistry PLC
Revision Y12 Chemistry PLC

... (f) the benefits of chlorine use in water treatment (killing bacteria) contrasted with associated risks (e.g. hazards of toxic chlorine gas and possible risks from formation of chlorinated hydrocarbons) Characteristic reactions of halide ions (g) the precipitation reactions, including ionic equation ...
Microsoft Word - Final Exam Study Guide
Microsoft Word - Final Exam Study Guide

... substitution reactions, SN1 mechanism, SN2 mechanism, alkene classifications, alkene stability, elimination reactions, Zaitsev’s rule, E1 mechanism, E2 mechanism, antiperiplanar, comparing substitution and elimination mechanisms, synthesis of ethers, alcohols, and epoxides, dehydration of alcohols, ...
Hydrocarbons Activity - Valley Catholic School
Hydrocarbons Activity - Valley Catholic School

... Period: _________ ...
CHE 106, F`95 E1(Word)
CHE 106, F`95 E1(Word)

... The sum of the masses of two hydrogen atoms (mass number 1) and two neutrons is 4.0330. Why does this differ from the mass of a helium atom (4.0026)? (a) (b) (c) (d) (e) ...
ch 4 powerpoint - not the powerpoint for fri ch_4_lecture
ch 4 powerpoint - not the powerpoint for fri ch_4_lecture

... Can form hydrogen bonds with water molecules, helping dissolve organic compounds such as sugars. ...
Hydrocarbons
Hydrocarbons

... and C - H bonds are nearly purely covalent) The O - H bond in a water molecule is highly polar due to the high electronegativity of oxygen ...
directed reading a
directed reading a

... a. what colors the atoms are b. how the atoms are connected c. how heavy the atoms are d. what size the atoms are _____ 4. What do the backbones of some compounds have hundreds or thousands of? a. carbon atoms c. structural formulas b. carbon molecules d. acid ions HYDROCARBONS AND OTHER ORGANIC COM ...
Introductory Chemistry: Concepts & Connections 4th Edition
Introductory Chemistry: Concepts & Connections 4th Edition

... is the same as the alkane with the -ane suffix changed to -ene. 2. Number the longest continuous chain starting from the end closest to the double bond. 3. Indicate the position of the attached alkyl groups by name and number. 4. If there are two or more of the same group attached to the chain, use ...
< 1 ... 121 122 123 124 125 126 127 128 129 ... 171 >

Haloalkane



The haloalkanes (also known, as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens. They are a subset of the general class of halocarbons, although the distinction is not often made. Haloalkanes are widely used commercially and, consequently, are known under many chemical and commercial names. They are used as flame retardants, fire extinguishants, refrigerants, propellants, solvents, and pharmaceuticals. Subsequent to the widespread use in commerce, many halocarbons have also been shown to be serious pollutants and toxins. For example, the chlorofluorocarbons have been shown to lead to ozone depletion. Methyl bromide is a controversial fumigant. Only haloalkanes which contain chlorine, bromine, and iodine are a threat to the ozone layer, but fluorinated volatile haloalkanes in theory may have activity as greenhouse gases. Methyl iodide, a naturally occurring substance, however, does not have ozone-depleting properties and the United States Environmental Protection Agency has designated the compound a non-ozone layer depleter. For more information, see Halomethane. Haloalkane or alkyl halides are the compounds which have the general formula ″RX″ where R is an alkyl or substituted alkyl group and X is a halogen (F, Cl, Br, I).Haloalkanes have been known for centuries. Chloroethane was produced synthetically in the 15th century. The systematic synthesis of such compounds developed in the 19th century in step with the development of organic chemistry and the understanding of the structure of alkanes. Methods were developed for the selective formation of C-halogen bonds. Especially versatile methods included the addition of halogens to alkenes, hydrohalogenation of alkenes, and the conversion of alcohols to alkyl halides. These methods are so reliable and so easily implemented that haloalkanes became cheaply available for use in industrial chemistry because the halide could be further replaced by other functional groups.While most haloalkanes are human-produced, non-artificial-source haloalkanes do occur on Earth, mostly through enzyme-mediated synthesis by bacteria, fungi, and especially sea macroalgae (seaweeds). More than 1600 halogenated organics have been identified, with bromoalkanes being the most common haloalkanes. Brominated organics in biology range from biologically produced methyl bromide to non-alkane aromatics and unsaturates (indoles, terpenes, acetogenins, and phenols). Halogenated alkanes in land plants are more rare, but do occur, as for example the fluoroacetate produced as a toxin by at least 40 species of known plants. Specific dehalogenase enzymes in bacteria which remove halogens from haloalkanes, are also known.
  • studyres.com © 2026
  • DMCA
  • Privacy
  • Terms
  • Report